Source: CURATED ×
Variant Gene DSI v DPI v Chr Position Consequence Alleles Class AF EXOME AF GENOME Num. diseases
rs112106319
TNC ; DELEC1
0.925 0.040 9 115094539 intron variant A/T snv 2.8E-03 3
rs112538845 0.925 0.040 4 184084475 downstream gene variant C/T snv 1.7E-02 3
rs113378111 1.000 0.040 2 9788024 intergenic variant G/A snv 2.8E-02 3
rs114465512
IGLV10-54
1.000 0.040 22 22047895 intron variant C/T snv 4.7E-03 3
rs117198528
LOC105372112
1.000 0.040 18 49694188 intergenic variant T/G snv 1.0E-02 3
rs11924809
DGKG
0.925 0.040 3 186353656 intron variant G/A snv 5.3E-02 3
rs12963463
TCF4
1.000 0.040 18 55431862 intron variant C/G;T snv 3
rs138472420
BICRA
1.000 0.040 19 47657765 intron variant G/A snv 3.3E-03 3
rs141746753 1.000 0.040 8 56934154 intergenic variant C/T snv 3.1E-03 3
rs142641502
CSTF3
0.925 0.040 11 33109861 intron variant T/C snv 8.0E-03 3
rs143405544
ADAMTS6
0.925 0.040 5 65459777 intron variant A/G snv 4.8E-03 3
rs143934587 0.925 0.040 20 19165806 intergenic variant G/A snv 9.1E-03 3
rs150175932
DCLK2
1.000 0.040 4 150101495 intron variant T/C snv 1.6E-02 3
rs1548076 0.925 0.040 15 69934284 intergenic variant G/A snv 0.95 3
rs1789891
ADH1B
1.000 0.080 4 99329262 intron variant C/A snv 0.13 3
rs182377406 0.925 0.040 11 67449378 upstream gene variant A/G snv 4.5E-04 3
rs183042538
ZHX3
0.925 0.040 20 41197420 intron variant A/T snv 3.2E-02 3
rs183124483
NLK
0.925 0.040 17 28110028 intron variant G/A snv 7.1E-04 3
rs188843168
ATP5MD
0.925 0.040 10 103390184 intron variant T/A;C snv 4.3E-04 3
rs189864513
LINC01618
0.925 0.040 4 52767390 intron variant T/C snv 1.9E-03 3
rs190783615 0.925 0.040 X 142772620 intergenic variant T/C snv 9.3E-03 3
rs1908557 0.925 0.040 4 89500202 intron variant T/C snv 0.31 3
rs1994321 1.000 0.040 11 12065766 upstream gene variant G/T snv 0.33 3
rs2251219
SMIM4 ; PBRM1
0.732 0.120 3 52550771 synonymous variant T/C;G snv 0.39; 4.0E-06 0.34 3
rs2435200
MAPT
0.925 0.080 17 45994485 intron variant G/A snv 0.40 3